期刊文献+

内质网应激与未折叠蛋白反应的研究进展 被引量:42

Endoplasmic reticulum and unfolded protein response
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摘要 目的:总结内质网应激与未折叠蛋白反应的国内外研究进展,阐述其分子机制和内质网应激相关性的细胞存活及凋亡途径。方法:应用PubMed及CNKI期刊全文数据库检索系统,以"内质网应激、未折叠蛋白反应、凋亡"为关键词,检索1990-01-2010-01相关内质网应激与未折叠蛋白反应等文献,最后纳入分析24篇。结果:内质网是真核细胞中重要的细胞器,是新合成跨膜蛋白和分泌蛋白折叠与成熟的加工厂。未折叠或错误折叠蛋白在内质网大量蓄积可以导致内质网应激,激活未折叠蛋白反应。未折叠蛋白反应是一种保守性细胞自我保护性措施,通过促进内质网对蓄积在网腔内的错误折叠或未折叠蛋白质的处理,使细胞功能恢复正常并使之存活;但是,过强或者持续时间过久的内质网应激可引起细胞凋亡。结论:内质网应激与未折叠蛋白反应的分子机制已比较清楚,但仍存在问题需进一步研究。 OBJECTIVE: To summarize the advances of domestic and foreign research on endoplasmic reticulum stress and unfolded protein response,to review its molecular mechanism and the pathways of the cell survival and apoptosis associated with endoplasmic reticulum stress.METHODS:The full text database of PubMed and CNKI were searched,and the words "endoplasmic reticulum stress/unfolded protein response/apoptosis" were used as Key words:.To retrieve the literature about endoplasmic reticulum stress and unfolded protein response from Jan.1990 to Jan.2010,and then 24 were used in analysis at last.RESULTS:The endoplasmic reticulum(ER),an important intracellular organelle of eukary-ocyte,is the factory for folding and maturation of newly synthesized transmembrane and secretory proteins.Accumulation of unfolded or misfolded proteins in ER leads to ER stress and triggers the unfolded protein response(UPR).UPR is a highly conserved self-protective mechanism by ameliorating the accumulation of unfolded or misfolded proteins in the ER;however if ER stress is severe or protracted,cell apoptosis may be induced.CONCLUSION:Though the molecular mechanism of endoplasmic reticulum stress and unfolded protein response is clear,there are still present some questions,and so it needs further study.
出处 《中华肿瘤防治杂志》 CAS 2010年第11期869-872,共4页 Chinese Journal of Cancer Prevention and Treatment
基金 国家自然科学基金(30870522)
关键词 内质网应激 未折叠蛋白反应 细胞凋亡 综述文献 endoplasmic reticulum stress unfolded protein response apoptosis review literature
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  • 1郭风劲,成军,宋方洲.X-盒结合蛋白1生物学功能研究进展[J].医学分子生物学杂志,2006,3(1):48-51. 被引量:3
  • 2Wu J, Kaufman RJ. From acute ER stress to physiological roles of the Unfolded Protein Response. Cell Death Differ, 2006,13:374-384.
  • 3Elida L, Tracy T Allen V. Endoplasmic reticulum stress: signaling the unfolded protein response. Physiology, 2007,22: 193-201.
  • 4Bertolotti A, Zhang Y, Hendershot LM, et al. Dynamic interaction of Bip and ER stress transducers in the unfolded protein response. Nat Cell Biol, 2000,2 : 326-332.
  • 5Hirota M, Kitagaki M, Itagaki H, et al. Quantitative measurement of spliced XBPlmRNA as an indicator of endoplasmic reticulum stress. J Toxicol Sci ,2006,31 : 149-156.
  • 6Kaufman RJ. Stress signaling from the lumen of the endoplasmic reticulum: coordination of gene transcriptional and translational controls. Genes & Development, 1999, 13 : 1211- 1233.
  • 7Wajant H, Pilzenmaier K Scheurich P. Tumour necrosis factor signaling. Cell Death Differ, 2003,10:45-65.
  • 8Beutler B, Cerami A. Cachectin and tumour necrosis factor as two sides of the same biological coin. Nature, 1986,320:584- 588.
  • 9Liu ZG, Han J. Cellular responses to tumor necrosis factor. Curr. Issues Mol. Biol. ,2001,3:79-90.
  • 10Lee K, Witoon T, Shen XH, et al. IREl-mediated unconventional mRNA splicing and S2P-mediated ATF6 cleavage merge to regulate XBPlin signaling the unfolded protein response. Genes & Develooment,2002,16:452-466.

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